Evidence map›Paper›PMID 32994778›Full record

ArticlePostepy dermatologii i alergologii2020

Efficiency of long-term high-dose intravenous ascorbic acid therapy in locally advanced basal cell carcinoma - a pilot study.

András Bánvölgyi, Kende Lőrincz, Norbert Kiss, Pinar Avci, Luca Fésűs, Róbert Szipőcs, Tibor Krenács, Nóra Gyöngyösi, Norbert Wikonkál, Sarolta Kárpáti and 1 more

Open access · goldAbstract read
In one paragraph

Article in Postepy dermatologii i alergologii, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

András BánvölgyiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Kende LőrinczDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Norbert KissDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Pinar AvciDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Luca FésűsDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Róbert SzipőcsR&D Ultrafast Lasers Ltd; Wigner RCP, Institute for Solid State Physics and Optics, Budapest, Hungary.
Tibor Krenács1 Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Nóra GyöngyösiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Norbert WikonkálDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Sarolta KárpátiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Krisztián NémethDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUWigner Research Centre for Physics · HUInstitute for Solid State Physics and Optics · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe anti-cancer properties of high-dose intravenous ascorbic acid have been demonstrated in various malignancies. In our recent study, we tested topically applied ascorbic acid to treat basal cell carcinoma (BCC), and achieved a good clinical response.

aimBased on these results, we decided to examine the efficacy and tolerability of high-dose intravenous ascorbic acid (IVA) for locally advanced BCC. MATERIAL AND

methodsIn this pilot study, patients diagnosed with locally advanced BCC who were not amenable to radiation, surgical or local therapy (no other treatment option was available at the time) received intravenous ascorbic acid (1-1.8 g/kg), in an outpatient setting, 1-3 times per week for a mean duration of 42 ±23.6 weeks. This therapy was generally well tolerated.

resultsAmong 4 patients who had a total of 165 (mean: 41 ±51, range: 1-114) skin lesions, 3 patients achieved stable disease and one had progressive disease. There was substantial variability in individual tumor response to therapy. With the aid of two-photon microscopy and second harmonic generation imaging techniques, alterations in collagen structure were observed between tumor nests during IVA therapy.

conclusionsOur results suggest that IVA is well tolerated in a small group of patients with extensive BCCs. However, in the era of smoothened (Smo) receptor inhibitors, it may only be considered as an adjuvant therapy in treatment-resistant cases.

Indexed as

ascorbic acidbasal cell carcinomavitamin C

Identifiers

PMID32994778
PMCPMC7507164
OpenAlexW2917349320

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.